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No correlation between androgen receptor CAG and GGN repeat length and the degree of genital virilization in females with 21-hydroxylase deficiency.
Welzel M, Schwarz HP, Hedderich J, Dörr HG, Binder G, Brämswig JH, Krude H, Richter-Unruh A, Niedziela M, Gromoll J, Krone N, Riepe FG, Holterhus PM. Welzel M, et al. Among authors: binder g. J Clin Endocrinol Metab. 2010 May;95(5):2443-50. doi: 10.1210/jc.2009-1338. Epub 2010 Mar 16. J Clin Endocrinol Metab. 2010. PMID: 20233785
Genotype-phenotype correlations in children and adolescents with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Dörr HG, Schulze N, Bettendorf M, Binder G, Bonfig W, Denzer C, Dunstheimer D, Salzgeber K, Schmidt H, Schwab KO, Voss E, Wabitsch M, Wölfle J. Dörr HG, et al. Among authors: binder g. Mol Cell Pediatr. 2020 Jul 9;7(1):8. doi: 10.1186/s40348-020-00100-w. Mol Cell Pediatr. 2020. PMID: 32647925 Free PMC article.
Experts' Opinion on the Prenatal Therapy of Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency - Guideline of DGKED in cooperation with DGGG (S1-Level, AWMF Registry No. 174/013, July 2015).
Dörr HG, Binder G, Reisch N, Gembruch U, Oppelt PG, Wieacker P, Kratzsch J. Dörr HG, et al. Among authors: binder g. Geburtshilfe Frauenheilkd. 2015 Dec;75(12):1232-1238. doi: 10.1055/s-0041-109717. Geburtshilfe Frauenheilkd. 2015. PMID: 28435171 Free PMC article.
297 results